Label: MOTION SICKNESS RELIEF- meclizine hydrochloride tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 12/14

If you are a consumer or patient please visit this version.

  • Active ingredient (in each tablet)

    Meclizine HCl 25 mg

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  • Purpose

    Antiemetic

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  • Uses

    prevents and treats nausea, vomiting, or dizziness associated with motion sickness

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  • Warnings

    Do not use

     for children under 12 years of age unless directed by a doctor.

    Ask a doctor before use if you have

    • glaucoma
    • difficulty in urination due to enlargement of the prostate gland
    • a breathing problem such as emphysema or chronic bronchitis 

    Ask a doctor or pharmacist before use if you are

     taking sedatives or tranquilizers.

    When using this product

    • do not exceed recommended dosage
    • drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careul when driving a motor vehicle or operating machinery 

    If pregnant or breast-feeding,

     ask a health professional before use.

    Keep out of reach of children.

     In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

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  • Directions

    • dosage should be taken one hour before travel starts
    • adults and children 12 years of age and over: take 1 to 2 tablets once daily or as directed by a doctor 
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  • Other information

    • protect from heat and humidity 
    • store at 25ºC (77F); excursions permitted between 15º-30ºC (59º-86ºF)
    • see end flap for expiration date and lot number 
    • for better identification keep tablets in carton until used
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  • Inactive ingredients

    corn starch, FD&C red #40 aluminum lake, lactose, magnesium stearate, raspberry flavor, silica gel, sodium saccharin

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  • Questions or comments?

     1-877-932-7948

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  • Principal Display Panel

    EQUALINE®

    NDC 41163-404-21

    compare to Bonine® Tablets active ingredient*

    motion sickness relief
    meclizine HCl 25 mg (antiemetic)

    raspberry flavored

    • causes less drowsiness
    • prevents motion sickness

    16 chewable tablets

    actual size

    *This product is not manufactured or distributed by Insight Pharmaceuticals, owner of the registered trademark Bonine® Chewable Tablets.
    50844    REV0712E40421

    DISTRIBUTED BY SUPERVALU INC.
    EDEN PRAIRIE, MN 55344 USA

    Contact us at 1-877-932-7948, or
    www.supervalu-ourownbrands.com

    TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

    Equaline 44-404

    Equaline 44-404

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  • INGREDIENTS AND APPEARANCE
    MOTION SICKNESS RELIEF 
    meclizine hcl tablet, chewable
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:41163-404
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MECLIZINE HYDROCHLORIDE (MECLIZINE) MECLIZINE HYDROCHLORIDE 25 mg
    Inactive Ingredients
    Ingredient Name Strength
    FD&C RED NO. 40  
    LACTOSE  
    MAGNESIUM STEARATE  
    Product Characteristics
    Color PINK Score 2 pieces
    Shape ROUND Size 10mm
    Flavor RASPBERRY Imprint Code 44;404
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:41163-404-21 2 in 1 CARTON
    1 8 in 1 BLISTER PACK; Combination Product Type = C112160
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part336 05/29/2002
    Labeler - SUPERVALU INC. (006961411)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(41163-404)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(41163-404)
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